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RE9 Advanced
RE9 Advanced - 42508-139-31 - (OCTISALATE, OCTOCRYLENE, and ZINC OXIDE)
Drug Information of RE9 Advanced
| Product NDC: | 42508-139 |
| Proprietary Name: | RE9 Advanced |
| Non Proprietary Name: | OCTISALATE, OCTOCRYLENE, and ZINC OXIDE |
| Active Ingredient(s): | 50; 80; 73.5 mg/mL; mg/mL; mg/mL & nbsp; OCTISALATE, OCTOCRYLENE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of RE9 Advanced
| Product NDC: | 42508-139 |
| Labeler Name: | Arbonne International, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100121 |
Package Information of RE9 Advanced
| Package NDC: | 42508-139-31 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (42508-139-31) > 30 mL in 1 BOTTLE, PUMP |
NDC Information of RE9 Advanced
| NDC Code | 42508-139-31 |
| Proprietary Name | RE9 Advanced |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (42508-139-31) > 30 mL in 1 BOTTLE, PUMP |
| Product NDC | 42508-139 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTISALATE, OCTOCRYLENE, and ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100121 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Arbonne International, LLC |
| Substance Name | OCTISALATE; OCTOCRYLENE; ZINC OXIDE |
| Strength Number | 50; 80; 73.5 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
